- Chapter 1: Structure and Bonding
- Chapter 10: Alkenes
- Chapter 11: Alkynes
- Chapter 12: Oxidation and Reduction
- Chapter 13: Mass Spectrometry and Infrared Spectroscopy
- Chapter 14: Nuclear Magnetic Resonance Spectroscopy
- Chapter 15: Radical Reactions
- Chapter 16: Conjugation, Resonance, and Dienes
- Chapter 17: Benzene and Aromatic Compounds
- Chapter 18: Electrophilic Aromatic Substitution
- Chapter 19: Carboxylic Acids and the Acidity of the OH Bond
- Chapter 2: Acids and Bases
- Chapter 20: Introduction to Carbonyl Chemistry; Organometallic Reagents; Oxidation and Reduction
- Chapter 21: Aldehydes and KetonesNucleophilic Addition
- Chapter 22: Carboxylic Acids and Their DerivativesNucleophilic Acyl Substitution
- Chapter 23: Substitution Reactions of Carbonyl Compounds at the ` Carbon
- Chapter 24: Carbonyl Condensation Reactions
- Chapter 25: Amines
- Chapter 26: CarbonCarbon Bond-Forming Reactions in Organic Synthesis
- Chapter 27: Carbohydrates
- Chapter 28: Amino Acids and Proteins
- Chapter 29: Lipids
- Chapter 3: Introduction to Organic Molecules and Functional Groups
- Chapter 30: Synthetic Polymers
- Chapter 4: Alkanes
- Chapter 5: Stereochemistry
- Chapter 6: Understanding Organic Reactions
- Chapter 7: Alkyl Halides and Nucleophilic Substitution
- Chapter 8: Alkyl Halides and Elimination Reactions
- Chapter 9: Alcohols, Ethers, and Epoxides
Organic Chemistry 3rd Edition - Solutions by Chapter
Full solutions for Organic Chemistry | 3rd Edition
atomic mass unit (amu)
A unit of measure equivalent to 1 g divided by Avogadro’s number.
Carbonyl group (Section 1.3C)
A C"O group.
The transfer of reactivity of an endgroup from one chain to another during a polymerization
A prefi x meaning on the same side
A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)
The minimum mass of fissionable material required to generate a self-sustaining nuclear chain reaction. (19.5)
A measure of radioactivity: 1 curie = 3.7 * 1010 nuclear disintegrations per second. (Section 21.4)
Stereoisomers that are not mirror images of one another.
In mass spectrometry, when the molecular ion breaks apart into fragments.
A law stating that the rate of effusion of a gas is inversely proportional to the square root of its molecular weight. (Section 10.8)
The SI unit for radiation dose
A reaction which involves the addition of a halogen and a hydroxyl group (OH) across an alkene.
A rule stating that electrons occupy degenerate orbitals in such a way as to maximize the number of electrons with the same spin. In other words, each orbital has one electron placed in it before pairing of electrons in orbitals occurs. (Section 6.8)
The energy required to separate completely the ions in an ionic solid. (Section 8.2)
A system for naming organic compounds.
Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons
Matter that has a fixed composition and distinct properties. (Section 1.2)
A six-membered cyclic hemiacetal form of a carbohydrate.
specific heat 1Cs2
The heat capacity of 1 g of a substance; the heat required to raise the temperature of 1 g of a substance by 1 °C. (Section 5.5)
For alkenes, a stereodescriptor that indicates that the two priority groups are on the same side of the p bond.